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CD27+ B cells in human lymphatic organs: re-evaluating the splenic marginal zone
Birte Steiniger1, Eva-Maria Timphus, Ralf Jacob
1Institute of Anatomy and Cell Biology, University of Marburg, Germany. steinigb@staff.uni-marburg.de
Immunology
|November 30, 2005
Summary
Human spleen marginal zones differ from rodents, with CD27(+) B cells found superficially in various lymphoid organs. This suggests a distinct recirculation compartment for B cells in humans, unlike in mice and rats.
Area of Science:
- Immunology
- Cell Biology
- Anatomy
Background:
- The marginal zone of human spleens has been considered a unique site for sessile memory B cells, based on rodent studies.
- This understanding is challenged by new findings on B cell distribution in human lymphoid tissues.
Purpose of the Study:
- To investigate the distribution and characteristics of CD27(+) B cells in human secondary lymphatic organs.
- To compare human splenic microanatomy with that of rodents.
- To propose a new hypothesis regarding B cell recirculation in humans.
Main Methods:
- In situ detection of CD27(+) B cells in human spleen, lymph nodes, appendix, tonsils, and terminal ilea.
- Analysis of B cell populations based on CD27 and Immunoglobulin D (IgD) expression.
- Comparative microanatomical analysis of human and rodent splenic white pulp.
Main Results:
- CD27(+) B cells are found in the superficial regions of B cell follicles in various human lymphoid organs, not exclusively in the spleen's marginal zone.
- A distinct microanatomical organization of the human splenic white pulp compared to rodents was identified.
- The follicular periphery in human secondary lymphatic organs appears to be a recirculation compartment for both naive and memory/natural reactive B cells.
Conclusions:
- The distribution of CD27(+) B cells suggests a fundamental difference between human and rodent splenic white pulp microanatomy.
- The follicular periphery in human secondary lymphatic organs may serve as a shared recirculation site for naive and memory B cells.
- Human and rodent B memory cells likely exhibit different recirculation behaviors.